Aesculap Implant Systems LLC 2022-08-10 Health serious FDA
Health · FDA · Recall #FDA-Z-1482-2022
PRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product… Recall
Issued August 10, 2022 · Aesculap Implant Systems LLC
In August 2022, Aesculap Implant Systems LLC recalled the PRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Endoscopic graspers may become separated at the weld from handle to the shaft of the device.
What you should do
- 1 Stop using PRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Aesculap Implant Systems LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Aesculap Implant Systems LLC
- Category
- Health
- Recall date
- August 10, 2022
- Units affected
- Not reported
- Sold at
- United States Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, M
- Recall number
- FDA-Z-1482-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Aesculap Implant Systems LLC has 4 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.